| Tag | Content |
|---|
EnhancerAtlas ID | HS081-09686 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr19:34310780-34312190 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf12 | MA0742.1 | chr19:34310995-34311010 | GGCCACGCCCTCCTG | + | 6.46 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_26999 | chr19:34310151-34312404 | Esophagus | | SE_32421 | chr19:34310338-34312371 | Gastric | | SE_54276 | chr19:34310171-34312632 | Spleen |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I033819 | chr19 | 34310149 | 34312946 |
|
Enhancer Sequence | CCTGCCCGCG GGAGAACCCA GGCCGCGCAT CCCTGGCTGG ACGGCGTCAC CAGCCGTAGC 60
TGGGCCAGGC CTGCTGCTCA AAGCCCGTGT CTAGGATGTC ACCAGAGCTC CCTTTTCTGT 120
GTCCTGGACC CGGTTCAGGG CCCCCGAGGA AGCTGCGGTT TGGGGCGAGC CGATTGCACC 180
AGCAGGGCCG GGCTGCTGCT CCCGGGGCTG ACGCGGGCCA CGCCCTCCTG GACGCGGACA 240
CACCCCCATT TCCCCGGGCC CACAGAGCCA CGCCTGGCCC TGCAGCCAAA CAGCGGGAAG 300
GCAGATTGGT ACGAGTAGGT ACAAGGCCCT GGAATTCTCG CCCGGTTGCC ACACACTGCA 360
CGGAGCATAA TTGGGGGAGG TTGTGCAACT GCCCGGGAAG CCGGGGCTCG CAACGAGGGC 420
TCTCTCCAAG TCCCCATCAC AGGCCTCCGG GGAGCCTCGG GACAGAGCCT GACGCCACCT 480
TCGGGTGACA TCGATGGCCT CGCTCTGGCA GAGGAGTAGT GTGGCTCTGC CGAGAACTGG 540
GGAGCCCGGG TCCCCGCAGG GCCAAGGGGA GGGAGGGCTG GCGGAAGGGG CCGCGCCCAC 600
AGCCCCAGGT GGCAGCAGCG GCGGTGGCGG TCCCGACTGG CAGAGCCTAA CGAGAACAGG 660
GCCTATCCCC AGGGGCCCCG GGCTGGACGC AGACCAGATC TCGCGGGGGT GGGCTGGGAG 720
GCGCCCGCCA GAGGCCGGAG GCTGACAGTG CCTTTCCTAT CCTATGGGTC TATTGTGGGC 780
CCGCGGAGCC CCCATGGGTG GGTCCATCCC CGGGCCCAGT GAGTCACTTC CCCAGGCCCC 840
GGAGGCCTTC GTGGAAGGTG CCTCCCTTTC CGGCAAAGCA TCCTTTGTTC TCCTGCTGGC 900
TTTGCTTCCC AATCCTCTCT GAGTTGCAAC CTTGAGGGTT TTAGGGGCAC CAAGCTCCCA 960
GGAGCACAGA GGTGGGCTTG GGTGCCACCT GGAGAGCGGG CTGCAGAAGG CTGCAGCTGC 1020
TTTTTTGCTT CCTCAGTTCC CTGCCCTCTC AAGGCCCAGG CTCTCCCACC TCCCCAGACG 1080
TCTGGGGAAA CCCACACTGC CCTGCATAGG TTGTGGTGTG CAGCCTCCGG ACTGCAGATC 1140
CTGAACGCGC ATCAGGAGGG AGGGAGGGAG GTTTCGATGC TCTCGCCCTG GCCAGCACCG 1200
CTCTGAGTTG CTGAACTGGC CTCAAGGCTT CTCTTGCATC AGGGAGAGGC TTCCGGCACC 1260
ACCACTGGCA CTCCTCCTTC TCCCTCCCTT TAGCCTCCCC CAGTTCCCAT GCCCAGGTGG 1320
AGGAACCCGT GTAGAAGCCC AGCCCAGGGA GGGAATTCAT CAAAGCACCT TCCCACACAG 1380
CCTCTAGTTT GCCTCCTCTC CACTCCCACC 1410
|
